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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559999Generated: October 26, 2026

2-Aminothiazole → 3-(2-Methyl-allyloxy)-4-nitrotoluene

https://huagongshe.com/reaction/559999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantMethallyl alcoholHCID 10557—
ReactantBenzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
Reactant4-Methyl-2-[(2-methylprop-2-en-1-yl)oxy]anilineHCID 45091245—
ProductHCID 59733018HCID 5973301870%
Product3-(2-Methyl-allyloxy)-4-nitrotolueneHCID 6035784475%

Reaction Steps

3-(2-Methyl-allyloxy)-4-nitrotoluene (0.78 g, 75%) was prepared from methallyl alcohol and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 4-methyl-2-(2-methyl-allyloxy)aniline (0.47 g, 70%) following general procedure B. 1-[4-Methyl-2-(2-methyl-allyloxy)-phenyl]-3-thiazol-2-yl-urea (210 mg, 70%) was prepared from 4-methyl-2-(2-methyl-allyloxy)aniline (179 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063081B2
Source datasetuspto-grants-2011_11
ORD IDord-bd8760d32a9945bdbdfea53e8eec5e4a
Source noteuspto-grants-2011_11